Wuxi Beien Surgery Device Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Wuxi Beien Surgery Device Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Disposable Endoscopic Staplers and Reload Unit, Disposable Hemorrhoidal Cutter Staplers, Disposable Linear Cutter Staplers, Disposable Circular Staplers
1
Total
1
Cleared
0
Denied
Wuxi Beien Surgery Device Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Wuxi, CN.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Wuxi Beien Surgery Device Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mid-Link Consulting Co, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Wuxi Beien Surgery Device Co., Ltd.
1 devices